Wheelchair Break Lever Extension

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Wheelchair Break Lever Extension FDA UDI
Generic Name: Wheelchair brake extension FDA UDI
Device Name: Wheelchair Break Lever Extension 11 inch; pair FDA UDI
Model / Reference: 10270 FDA UDI
Description: Wheelchair Break Lever Extension 11 inch; pair FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784027012 FDA UDI
FDA Product Code: KNO FDA UDI
GMDN Term: Wheelchair brake extension FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

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Expiration Date

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Manufacturing Date

FDA UDI

Category: Wheelchair brake extension

Wheelchair Break Lever Extension by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Wheelchair Break Lever Extension — Dynarex Corp. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dynarex Corp.

Sources (1)

FDA UDI 5cd74480-714e-40df-9447-aad5129e4928 33 fields · synced May 30, 2026